Colon Cancer: Gene >> SNW1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261531
Start	77737056:77737056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.553G>A
AA Mutation	p.Gly185Arg(p.G185R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261531
Start	77738832:77738832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.479C>T
AA Mutation	p.Ala160Val(p.A160V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261531
Start	77751395:77751395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759186141
CDS Mutation	c.254C>T
AA Mutation	p.Ala85Val(p.A85V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261531
Start	77723259:77723259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1052A>C
AA Mutation	p.Glu351Ala(p.E351A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261531
Start	77732493:77732493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.883G>A
AA Mutation	p.Asp295Asn(p.D295N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261531
Start	77738991:77738991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.401G>T
AA Mutation	p.Arg134Met(p.R134M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261531
Start	77732524:77732524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148781957
CDS Mutation	c.852C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261531
Start	77751405:77751405(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.244delA
AA Mutation	p.Met82CysfsTer44(p.M82Cfs*44)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261531
Start	77731086:77731087(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.934dupA
AA Mutation	p.Met312AsnfsTer10(p.M312Nfs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261531
Start	77732595:77732596(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.780_781insTTTAAAAGTA
AA Mutation	p.Thr261PhefsTer14(p.T261Ffs*14)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SNW1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261531
Start	77739009:77739009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.383A>G
AA Mutation	p.Asp128Gly(p.D128G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript